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How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Design your service using GOV.UK styles, components and patterns.
How to conform with the legal requirements for placing medical devices on the market.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Advice on writing clear notices and maximising replies to your FSNs.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Details of General Licences issued by OFSI
Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Find news, information and advice from the government on starting or growing your business.
Apply for a higher education course, track your application and accept or reject your offers.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Find the address, contact details and opening times of the UK visa application centre for your country.
Find registered patents, patent applications and pending patents
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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